Intrathecal Morphine and Post-Operative Pain Relief in Robotic Surgeries: A Systematic Review and Meta-Analysis

Despite the potential benefits of intrathecal morphine (ITM), the precise role and dosing of ITM in robotic assisted surgery (RAS) remains unclear. This systematic review explores real-world evidence to evaluate the efficacy and outcomes of ITM in patients undergoing RAS. In accordance with PRISMA guidelines, a comprehensive search was conducted on four databases: MEDLINE, Embase, Cochrane Library and APA PsycInfo. Primary outcomes included pain scores at rest and on exertion at 24- and 48-h time intervals, and secondary outcomes aimed to explore the side effects of ITM. A meta-analysis was conducted to determine mean differences. A risk of bias assessment was conducted via the Cochrane Risk of Bias 2 tool. A total of 9 RCTs involving 619 patients were included in this review, of which 298 patients were administered ITM. Significant pain score reductions were observed both at rest (MD = −27.15; 95% CI [−43.97, −10.33]; I2 = 95%; p = 0.002) and on exertion (MD = −25.88; 95% CI [−37.03, −14.72]; I2 = 79%; p = 0.0003) 24 h postoperatively in the ITM groups, accompanied by a notable decrease in postoperative IV morphine equivalent consumption at 24 h (MD = −20.13; 95% CI [−30.74, −9.52]; I2 = 77%; p = 0.0002). ITM improved pain scores both at rest and on exertion at 24 and 48 h intervals, concurrently reducing the need for postoperative opioid consumption, but at the cost of an increased incidence of adverse events.


Introduction
Current postoperative pain management strategies like opioids carry risks of adverse effects and inadequate pain relief.This can lead to delayed mobilisation, chronic pain development, and extended hospital stays [1].
Morphine is an opioid administered for acute and chronic pain conditions [2].As an affordable, effective, and well-tolerated analgesia, morphine is often used for postoperative pain management, either via oral (PO), intravenous (IV), subcutaneous (SC), intramuscular (IM) or intrathecal (commonly described as spinal) routes.However, administration of PO and IV morphine remains challenging since, sometimes, a larger amount of morphine is required to achieve an analgesic effect.Consequently, patients are at a greater risk of side effects such as nausea and vomiting.SC and IM morphine routes have been shown to have a time delay in analgesic effects in the immediate postoperative period [3].
Delivered via the intrathecal or subarachnoid space in the lower lumbar levels, intrathecal morphine (ITM) directly interacts with opioid receptors (mu, delta and kappa) and ion channels located in the dorsal horn of the spinal cord [2,4].This leads to an overall decrease in the release of excitatory transmitters and an increase in inhibitory transmitters within pain pathways.Therefore, nociceptive pain signals are significantly reduced [5].Moreover, ITM administration in the cerebrospinal fluid allows for bypass of first-pass metabolism and the blood-brain barrier [6].As a result, analgesic effects from ITM can be achieved at a lower dose with fewer adverse effects, together with a longer duration of action that lasts up to 20 h [2].Correspondingly, ITM is an increasingly accepted form of perioperative and postoperative analgesia.
First described by Wang et al. in 1979, ITM was successfully utilised in patients with genitourinary tract malignancies [7].Subsequently, ITM is indicated for pain management in various surgeries [8].
Despite present pain management guidelines surrounding the risk/benefit ratio of ITM, its efficacy and safety in robotic-assisted procedures remain unclear.Prior studies have had small sample sizes and inconsistent results on optimal dosing to balance analgesia and side effects [9,10].Given that ITM has the potential to improve postoperative RAS outcomes, we aimed to systematically review the available evidence on ITM for postoperative pain management in robotic surgery.Our objectives were to assess its effects on pain scores, opioid use and adverse events compared to other analgesia techniques.

Materials and Methods
This systematic review was performed in accordance with the Preferred Reporting Items for Systematic Review and Meta-analysis (PRISMA-P) guidelines and was registered in the International Prospective Register of Systematic Reviews (PROSPERO) (CRD42023405398) [11].
We searched Pubmed, Embase, Cochrane Library and PsyInfo using defined search terms for relevant randomised controlled trials.The search was last performed on 11 March 2023.We utilised the online platform Rayyan QCRI to perform deduplication and screening of papers via title and abstract independently [12].A full-text review was subsequently conducted for final inclusion into our systematic review while adhering to our selection criteria.Two authors (Z.H.T. and E.T.) independently screened records and extracted data on study characteristics, patient demographics, ITM dosing, spinal anaesthesia details, control analgesia and key outcomes.Any conflicts were resolved by consensus or appeal to the senior author (P.F.).

Selection Criteria
Utilising the Populations, Interventions, Comparators and Outcomes (PICO) framework from the Cochrane Handbook of Systematic Reviews, we selected studies based on the following inclusion criteria: (a) RCTs/ongoing RCTs of adult patients (≥18 years old) undergoing robotic/robot-assisted surgeries with administration of ITM, (b) comparison of any other analgesia/anaesthetic techniques apart from ITM or placebo/saline control groups, and (c) inclusion of pain scores, opioid consumption by patients and any adverse drug reactions [13].
Studies with paediatric patients were excluded.Studies reporting minimally invasive surgeries were excluded.Non-english studies, non-RCTs, as well as animal studies were excluded.Our inclusion and exclusion criteria can be found in the PICO table (Table 1).

Data Extraction and Quality Assessment
A data sheet was utilised to extract relevant data from our included studies.Primary outcomes analysed were pain scores on a 0-100 VAS at 24 and 48 h and opioid consumption at 24 h in morphine equivalents.Secondary outcomes analysed were adverse event rates at a 24 h time interval.
We defined the primary outcome of interest in accordance with the British Pain Society and Faculty of Pain Medicine guidelines [14].These include the verbal rating scale, a visual analogue scale or a numerical rating scale.A questionnaire developed by the British Pain Society requires patients to score their pain on a scale of 1-10 to classify the intensity of their pain.Studies that reported Numeric Rating Scale (NRS) pain scores from 11 (0-10) or 10 (1-10) point scales were transposed to a 0 (no pain)-100 (worst imaginable pain) Visual Analogue Scale (VAS) scale.For studies that presented pain scores categorised as mild, moderate and severe, the mean score within each category was extracted and transposed to the VAS scale.The PROSPECT methodology suggests a mean difference of 10 mm on a VAS scale should be considered a statistically significant effect [15].As such, a statistically significant difference in effect size of >10.0 was considered to be clinically relevant in the meta-analysis.
All postoperative opioid and rescue analgesic consumption at 24 h were converted to IV morphine equivalent, where the dose equivalent is defined as follows: 100 µg IV fentanyl = 100 mg IV tramadol = 100 mg IV pethidine = 10 mg IV morphine [16,17].
The secondary outcome aims to explore side effects such as nausea, vomiting, pruritus, urinary retention, constipation and respiratory depression at 24 h, postoperatively.Nausea is defined as an unpleasant sensation of needing to vomit, which can be accompanied by autonomic symptoms such as salivation, pallor, tachycardia and hidrosis [18].Vomiting is the ejection of the contents from the stomach through the mouth [19].Pruritus is defined as severe itching of the skin coupled with the desire to scratch [20].Urinary retention is defined as the inability to voluntarily pass an adequate volume of urine [21].Constipation is defined as a reduction in the frequency or difficulty of evacuating stools [22].Opioidinduced respiratory depression is defined as SaO 2 <94% and/or PaCO 2 >6 kPa, or a respiratory rate <6 breaths per min [23].

Risk of Bias Assessment
Studies were evaluated for a risk of bias using the Cochrane Risk of Bias 2 (RoB2) tool across 5 domains [24].Each study was assessed twice by two independent reviewers.Any discrepancies were resolved through discussion with the senior author.Each domain was assessed as "high risk", "some concerns" or "low risk" with the inclusion of an overall risk of bias.

Statistical Analysis
Data were presented as percentages with raw values or means ± the standard deviation unless otherwise indicated.For studies that did not present in the above format, we attempted to contact the corresponding authors for access to the relevant data or complete dataset.If there were no responses, data presented as the median (IQR) was approximated as the mean ± the standard deviation, where the median was estimated as the mean and the standard deviation as the IQR divided by 1.35.
Meta-analyses of all listed outcomes were conducted on Review Manager [RevMan Version 5.4] software (Cochrane Collaboration, Copenhagen, Denmark).Due to high heterogeneity, the random effects model was used for a pooled meta-analysis of continuous variables with the effect sizes, 95% confidence interval and p values calculated to signify statistical significance.Heterogeneity was assessed with I 2 values and Cochran's Q test, where <50% represented low heterogeneity and ≥50% represented substantial heterogeneity [25].
Sub-analyses were conducted based on the surgical procedure according to primary and secondary outcomes.Sensitivity analyses were performed, excluding individual studies and controlling for ITM-only spinal anaesthesia.Publication bias was visually interpreted via funnel plots for each time point (24 and 48 h) for pain scores at rest and on exertion [26].

Search Results
A total of 31 studies were identified, of which 16 studies were screened for full-text review after removal of duplicates and exclusion via title and abstract.Of the 16 studies, 7 studies were excluded.Reasons for exclusion are as follows: surveys, conference case reports, invited commentary or unable to extract postoperative outcomes.Quality assessment was performed on all nine included studies using the Cochrane Rob2 tool, and no study was excluded after quality assessment [9,[27][28][29][30][31][32][33][34] (Figure 1).

Study Characteristics
All included studies were published between 2013 and 2023 and were from six different countries (Israel, Italy, Republic of Korea, The Netherlands, Sweden and USA).Types of robotic procedures include prostatectomy, nephrectomy, hysterectomy, sacrocolpopexy and coronary artery bypass.A total of 619 patients were included, of which 298 patients were in the ITM group and 321 patients were in the control group.

Study Characteristics
All included studies were published between 2013 and 2023 and were from six different countries (Israel, Italy, Republic of Korea, The Netherlands, Sweden and USA).Types of robotic procedures include prostatectomy, nephrectomy, hysterectomy, sacrocolpopexy and coronary artery bypass.A total of 619 patients were included, of which 298 patients were in the ITM group and 321 patients were in the control group.
Within the included studies, the dose of ITM ranged from 0.10 mg to 0.50 mg.The use of spinal anaesthesia was reported across five studies, where all studies reported the use of bupivacaine except Segal et al., 2013, who reported the use of fentanyl [32].The types of controls ranged from sham procedure, normal saline and other anaesthetic agents such as IV fentanyl and propofol, IV morphine, IV-PCA (fentanyl, ketorolac and ramosetron), IV tramadol, TAP block with ropivacaine, and oral oxycodone.The study characteristics are summarised in Table 2.

Pain Scale Methods
All nine studies reported pain scores using either the Numeric Rating Scale (NRS) or Visual Analogue Score (VAS).The majority of the studies reported both pain at rest and on exertion, except Koning et al., 2020 [9], which reported pain on exertion and Chae et al., 2022 [28], that reported pain at rest.Pain scores at rest or on exertion were not specified in Engström et al., 2023 [30].All studies specified time intervals at which the pain scores were measured except Engström et al., 2023 [30].

Pain Scores on Rest and after Exertion after Postoperative ITM at 48 h
A total of four studies reported pain scores 48 h postoperatively [27][28][29]32].Of which, two studies reported lower pain scores on both categories in the ITM group.Only Segal et al., 2013 [32], reported higher pain scores in the ITM group compared to the control group at rest and on exertion.Pain scores at rest and on exertion were not specified in Chae et al., 2022 [28], and pain scores on exertion were not specified in Dhawan et al., 2021 [29] (Table 3).

Postoperative Consumption of Equivalent IV Morphine Consumption at 24 h
A total of four studies were observed to have a reduction in postoperative IV morphine equivalent consumption at 24 h in the ITM groups [27,29,32,34] (Table 3).Except for Bae et al. [27] due to missing data, the meta-analysis of three studies found that ITM reduced 24 h IV morphine equivalent consumption (MD = −20.13;95% CI [−30.74,−9.52]).Statistical heterogeneity is considerable at I 2 = 77%, and Cochran's Q test revealed p = 0.0002 (Figure 4).

Pain Scores on Rest and after Exertion after Postoperative ITM at 48 h
A total of four studies reported pain scores 48 h postoperatively [27][28][29]32].Of which, two studies reported lower pain scores on both categories in the ITM group.Only Segal et al., 2013 [32], reported higher pain scores in the ITM group compared to the control group at rest and on exertion.Pain scores at rest and on exertion were not specified in Chae et al., 2022 [28], and pain scores on exertion were not specified in Dhawan et al., 2021 [29] (Table 3).

Postoperative Consumption of Equivalent IV Morphine Consumption at 24 h
A total of four studies were observed to have a reduction in postoperative IV morphine equivalent consumption at 24 h in the ITM groups [27,29,32,34] (Table 3).Except for Bae et al. [27] due to missing data, the meta-analysis of three studies found that ITM reduced 24 h IV morphine equivalent consumption (MD = −20.13;95% CI [−30.74,−9.52]).Statistical heterogeneity is considerable at I 2 = 77%, and Cochran's Q test revealed p = 0.0002 (Figure 4).

Nausea and Vomiting
A total of four studies reported an increased incidence of nausea in the ITM groups, ranging from 22.2% to 36.4% [29,31,33,34].Use of antiemetics as prophylaxis and/or treatment was also reported across eight studies [9,[30][31][32][33][34]. Bae et al., 2017 [27], reported no difference in the incidence of nausea, though two patients in the control group required 10 mg of metoclopramide.Prophylaxis of nausea and vomiting included ondansetron,

Secondary Outcomes 3.4.1. Nausea and Vomiting
A total of four studies reported an increased incidence of nausea in the ITM groups, ranging from 22.2% to 36.4% [29,31,33,34].Use of antiemetics as prophylaxis and/or treatment was also reported across eight studies [9,[30][31][32][33][34]. Bae et al., 2017 [27], reported no difference in the incidence of nausea, though two patients in the control group required 10 mg of metoclopramide.Prophylaxis of nausea and vomiting included ondansetron, dehydrobenzperidol, ramosetron and betamethasone, while treatment included ondansetron, dehydrobenzperidol and metoclopramide.Likewise, four studies reported an increased incidence of vomiting in the ITM groups, ranging from 0% to 20% [27,29,33,34].More information can be found in Table S1.

Urinary Retention
Engstrom et al., 2023 [30], was the only study to note a higher incidence of urinary retention (6.52%, n = 3) in the ITM group as opposed to the control group (4.17%, n = 2); however, it is not possible to determine the statistical significance of this finding due to

Urinary Retention
Engstrom et al., 2023 [30], was the only study to note a higher incidence of urinary retention (6.52%, n = 3) in the ITM group as opposed to the control group (4.17%, n = 2); however, it is not possible to determine the statistical significance of this finding due to the small study numbers.Notably, Dhawan et al., 2021 [29], documented a urinary retention rate of 2.7% (n = 1) in the control group, whereas no patients in the ITM group experienced this issue.Segal et al., 2013 [32], reported no difference in urinary retention in either the control or the ITM groups (Table S1).

Respiratory Depression
Amongst the studies which reported the incidence of respiratory depression, five studies found no incidence of respiratory depression events in either the control or the ITM groups [27,[29][30][31]34] (Table S1).

Quality Assessment and Risk of Bias
Using the Cochrane Rob2 Tool, studies were investigated for bias by two independent researchers [24].Any discrepancies were resolved through discussion.Bias was evaluated under five domains and was assessed to have a low risk, some concerns or a high risk of bias.A summary of our risk of bias assessment can be found in Figure 6.evaluated under five domains and was assessed to have a low risk, some concerns or a high risk of bias.A summary of our risk of bias assessment can be found in Figure 6.
Russo et al., 2022 [31], did not report their randomisation process and did not specify if participants, clinicians and researchers were blinded during the trial.However, there were no significant differences in the baseline characteristics between the intervention and control groups, thus we evaluated the study to be of some concerns in bias.
Pain scores were measured every 30 min until discharge in Segal et al., 2013 [32].However, pain scores were only reported in the recovery unit, postoperative day 1 and postoperative day 2.This highlights a high risk of bias as the reported results could have been selected on the basis of results.

Test for Statistical Heterogeneity
Multiple instances were detected where the removal of one study changed the results of an analysis from statistically insignificant to statistically significant for primary outcomes exploring pain scores on rest at 24 h time intervals and secondary outcomes, with the exception of Shim et al., 2021 [34], and Russo et al., 2022 [31], respectively.The sensitivity analysis of the studies did not find any evidence of a significant change in the analysis for reported primary outcomes with regards to pain scores on exertion at 24 h time intervals.Exclusion of studies with a high risk of bias did not find any significant changes in the reported primary outcomes.
Sensitivity analysis was attempted after excluding all studies not including "basic analgesics" in both groups, where "basic analgesics" is defined as the regular or documented use of paracetamol and any NSAIDs not only as rescue analgesia but as regularly/systematically prescribed or documented/quantified in the studies.Due to missing data in Russo et al., 2022 [31], three studies were identified, and sensitivity analysis was Russo et al., 2022 [31], did not report their randomisation process and did not specify if participants, clinicians and researchers were blinded during the trial.However, there were no significant differences in the baseline characteristics between the intervention and control groups, thus we evaluated the study to be of some concerns in bias.
Pain scores were measured every 30 min until discharge in Segal et al., 2013 [32].However, pain scores were only reported in the recovery unit, postoperative day 1 and postoperative day 2.This highlights a high risk of bias as the reported results could have been selected on the basis of results.

Test for Statistical Heterogeneity
Multiple instances were detected where the removal of one study changed the results of an analysis from statistically insignificant to statistically significant for primary outcomes exploring pain scores on rest at 24 h time intervals and secondary outcomes, with the exception of Shim et al., 2021 [34], and Russo et al., 2022 [31], respectively.The sensitivity analysis of the studies did not find any evidence of a significant change in the analysis for reported primary outcomes with regards to pain scores on exertion at 24 h time intervals.Exclusion of studies with a high risk of bias did not find any significant changes in the reported primary outcomes.
Sensitivity analysis was attempted after excluding all studies not including "basic analgesics" in both groups, where "basic analgesics" is defined as the regular or documented use of paracetamol and any NSAIDs not only as rescue analgesia but as regularly/systematically prescribed or documented/quantified in the studies.Due to missing data in Russo et al., 2022 [31], three studies were identified, and sensitivity analysis was performed on pain scores on exertion after postoperative ITM at 24 h [9,33,34].Revised sensitivity analysis revealed a significant improvement in pain scores in the ITM group (MD = −17.05;95% CI [−23.24,−10.86]).Statistical heterogeneity is low at I 2 = 0%, with Cochran's Q test yielding p < 0.00001 (Figure S1).

Publication Bias
The funnel plot was based on the chosen outcome with the highest number of studies, i.e., pain scores on exertion after postoperative ITM at 24 h.Visual analysis of the funnel plot did not allow us to confirm any risk of publication bias (Figure S2).
However, benefits must be weighed against increased postoperative side effects.For the purposes of this review, the side effects that were noted in the selected trials include nausea, vomiting, pruritus and respiratory depression.Based on our results, there is an increased incidence of nausea (MD = 2.61; 95% CI [1.07, 6.37],I 2 = 0%, p = 0.03) and pruritus (MD = 9.96; 95% CI [1.32, 75.30],I 2 = 0%, p = 0.03) at 24 h time intervals.Although respiratory depression is the most serious adverse side effect of ITM, there was no incidence of respiratory depression events found in either the ITM or the control groups [27,29,30,32,35].This may be due to the dose of ITM utilised ranging from 0.10 mg to 0.50 mg, highlighting the dose dependent relationship between ITM and respiratory depression.Though greater analgesic effects can be achieved with higher doses of ITM (>500 µg), it is also associated with significant adverse events, most notably respiratory depression [37][38][39].The insufficient studies available meant that we were unable to conduct a meaningful analysis of the dose-dependent relationship between ITM and different robotic procedures.
Due to the heterogeneity of the reported secondary outcomes, a meaningful comparison could only be made for papers that reported side effects post 24 h via metaanalysis [31,33,34].Another limitation in our data collection is the documentation of nausea and vomiting as a collective measure rather than individual occurrences in Russo et al., 2022 [31], of which we assumed all patients to have nausea.Most studies only included patients with an ASA status of 1-2, which makes the incidence of other well-known ITM side effects such as haemodynamic hypotension, headaches and seizures difficult to determine, especially in high-risk patients [3].The use of antiemetics postoperatively such as metoclopramide and ondansetron in some studies can mask the incidence of postoperative nausea and vomiting, which may be underreported [9,27,31].
Only four studies reported the use of regular basic analgesics in both ITM and control groups as per the PROSPECT guideline methodology [9,31,33,34].Alignment of routine clinical practice allows an accurate assessment of ITM and the ability to determine if ITM provides additional pain relief on top of basic analgesics with or without locoregional analgesia in the overall pain management strategy.As a result, the sensitivity analysis is limited to only three studies reporting pain scores on exertion after postoperative administration of ITM at 24 h (MD = −17.05;95% CI [−23.24,−10.86];I 2 = 0%; p < 0.00001).A recommendation for future research is to conduct studies with basic analgesics in both arms for pain scores at rest and on exertion at different time intervals.
Robotic surgery has been an increasingly popular surgical approach since its establishment in 1979.Since then, over 10 million procedures have been performed worldwide, with an increase from 1.8% to 15.1% across all general surgical procedures in Michigan alone from 2012 to 2018 [40,41].However, the advent of RAS remains relatively new, with a lack of clear established guidelines in the context of postoperative pain management.As a derivative of laparoscopic surgery, postoperative pain in RAS is associated with several underlying mechanisms: incisional port site pain, pneumoperitoneum and referred pain [42].CO 2 insufflation in the peritoneum leads to shearing of blood vessels, traction on nerve endings and release of inflammatory mediators.Residual gas within the peritoneal cavity induces diaphragmatic stretching and irritation of the phrenic nerve, resulting in shoulder, abdominal or back pain [43].Furthermore, patients undergoing RAS are required to be positioned at a steeper angle, i.e., the Trendelenburg position, which increases the risk of positional injuries and synergistic complications of pneumoperitoneum and referred pain.However, postoperative visceral pain following RAS is often short-lived and typically resolves within 24 h.When combined with the extended analgesic benefits of ITM lasting up to 20 h, ITM may prove to be a valuable postoperative analgesic intervention for RAS.
It should be noted that most included studies remain heterogeneous with different follow-up time periods and reported pain scales.Limitations include clinical and moderate heterogeneity between studies, small sample sizes and a lack of long of long-term followups.As a result, our statistical analysis was limited to studies that reported pain outcomes at 24 h and 48 h, postoperatively.Moreover, most studies did not adhere to definitions for pain scales according to ACTTION, where traditional pain scales such as NRS or VAS pain scales are defined as 0-10 and 0-100, respectively [44].To have a meaningful analysis of pain scores from our included studies, we adapted pain scales to the VAS pain scale for standardisation.Furthermore, limited studies for postoperative equivalent IV morphine consumption at a 24 h time interval prevented us from making a meaningful analysis among different robotic procedures.Subgroup analysis for primary outcomes could only be localised to RALP studies due to the lack of studies in other robotic procedures.Due to the paucity of studies that included basic analgesics with or without locoregional anaesthesia in both ITM and control groups, the sensitivity analysis was also limited to pain scores on exertion after postoperative ITM at 24 h.

Conclusions
Our study demonstrates that ITM improved pain scores at rest and on exertion at 24 h and 48 h time intervals with reduced postoperative opioid equivalent consumption.However, pain management in most studies was not PROSPECT compliant, in particular to the systematic use of non-opioids.To accurately assess the true effectiveness of ITM in RAS, future large RCTs should compare ITM to alternative active comparators, intravenous morphine bolus administered under general anaesthesia, or combinations with locoregional analgesics in specific robotic procedures with the standardisation of protocols and outcomes.Cost effectiveness studies are needed to determine whether reduced opioid use offsets increased risks of ITM side effects.Overall, ITM holds promise as an opioid-reducing adjuvant, but optimal patient selection and dosing requires further research.

Future Development/Gaps
This study highlights the need for further research into the prospects of employing alternative perioperative analgesia protocols in specific RAS procedures to allow for the standardisation of analgesic techniques.Furthermore, a standardised pain evaluation tool also needs to be developed to facilitate a better understanding of the variation of the perception of pain in different patients.

Figure 3 .
Figure 3. Pain scores on exertion after postoperative ITM at 24 h [9,27,29,32-34].3.3.4.Pain Scores on Rest and after Exertion after Postoperative ITM at 48 hA total of four studies reported pain scores 48 h postoperatively[27][28][29]32].Of which, two studies reported lower pain scores on both categories in the ITM group.Only Segal et al., 2013[32], reported higher pain scores in the ITM group compared to the control group at rest and on exertion.Pain scores at rest and on exertion were not specified in Chae et al., 2022[28], and pain scores on exertion were not specified in Dhawan et al., 2021[29] (Table3).3.3.5.Postoperative Consumption of Equivalent IV Morphine Consumption at 24 h A total of four studies were observed to have a reduction in postoperative IV mor-

Table 1 .
Inclusion and exclusion criteria for selection criteria of studies.

Table 2 .
Overview of included studies.
Legend: CABG Coronary Artery Bypass Graft, ITM Intrathecal Morphine, NR not reported, RALP Robot-Assisted Laparoscopic Prostatectomy, TAP Transversus Abdominal Plane, USA United States of America.Continuous data are presented as absolute values unless otherwise stated.*Value represented as mean ± standard deviation.†Value represented as range only.

Table 3 .
Primary outcomes of included studies.
Legend: ITM Intrathecal Morphine, IV-PCA Intravenous Patient Controlled Analgesia, NR not reported, TAP Transversus Abdominal Plane.Continuous data are presented as mean ± standard deviations unless stated otherwise.* Value represented as absolute values.